7Goto Y, Tojo M, Tohyama J, et al. A novel point mutation in the mitochondfial tRNA (Leu) (UUR) gene in a family with mitochondrial myopathy. Ann Neurol, 1992, 31: 672-675.
8McDonnell MT, Schaefer AM, Blakely EL, et al. Noninvasive diagnosis of the 3243A > G mitochondrial DNA mutation using urinary epithelial ceils. Eur J Hum Genet, 2004, 12: 778-781.
9Kauimann P, Engelstad K, Wei Y, et al.Natural history ol MELAS associated with mitochondrial DNA m. 3243A > G genotype. Neurology, 2011, 77 : 1965-1971.
10Sharma LK, Lu J, Bai Y. Mitochondrial respiratory complex I: structure, function and implication in human diseases. Curr Med Chem, 2009, 16: 1266-1277.
6Burrage LC, Tang S, Wang J, et al. Mitochondrial myopathy, lactic acidosis, and sideroblastic anemia (MLASA) plus associated with a novel de novo mutation (m.8969G > A) in the mitochondrial encoded ATP6 gene[J]. Mol Genet Metab, 2014, 113(3): 207-212. DOI: 10.1016/j.ymgme.2014.06.004.
7Aurangzeb S, Vale T, Tofafis G, et al. Mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS) in the older adult[J]. Pratt Neurol, 2014, 14(6): 432-436. DOI: 10.1136/practneurol-2014-000853.
8Gieraerts C, Demaerel P, van Damme P, et al. Mitochondrial eneephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome mimickingherpes simplex encephalitis on imaging studies[J]. J Comput Assist Tomogr, 2013, 37(2): 279-281. DOI: 10.1097/RCT.0b013e3182811170.
9Steriade C, Andrade DM, Faghfoury H, et al. Mitochondrial encephalopathy with lactic acidosis and stroke-like episodes (MELAS) may respond to adjunctiveketogenic diet[J]. Pediatr Neurol, 2014, 50(5): 498-502. DOI: 10.1016/j.pediatmeurol. 2014. 01.009.
10Chaudhry N, Patidar Y, Puri V. Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes unveiled by valproate[J]. J Pediatr Neurosci, 2013, 8(2): 135-137. DOI: 10.4103/1517-1745.117847.